A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897599



Internal ID22672703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168830019..168830311hg38UCSC Ensembl
chr4:169751170..169751462hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420231
Samples
Known GenesPALLD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897599
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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